Author

Kitchener D. Wilson

Stanford Cardiovascular InstituteORCID 0000-0002-6351-3220Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Developmental Biology· 1 Genomics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:differential expression· 2 Organism:human· 2 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Approach:deep learning· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Assay:scATAC-seq· 1

Frequent Co-Authors

Ioannis KarakikesiD· 2 shared Joseph C. WuiD· 2 shared Mengcheng SheniD· 2 shared Abhimanyu BanerjeeiD· 1 shared Akshay BalsubramaniiD· 1 shared Angello Huerta Gomez· 1 shared Anna ShcherbinaiD· 1 shared Anshul Bharat KundajeiD· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersDevelopmental Biology

Ioannis KarakikesORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Developmental BiologySciencePeer-reviewedJun 5, 2025

Micropatterned Organoids Enable Modeling of the Earliest Stages of Human Cardiac Vascularization

Oscar John Abilez, Huaxiao Yang, Yuan Guan…·Joseph C. Wu

The paper demonstrates that micropatterned human pluripotent stem cells can model early human cardiac vascularization in vitro, resembling a 6.5 post-conception week heart and revealing conserved vascular development programs.

95 citationstop 1%

humanscRNA-seq

𝕏 PostBluesky

GenomicsCellPeer-reviewedDec 1, 2022

Integrative single-cell analysis of cardiogenesis identifies developmental trajectories and non-coding mutations in congenital heart disease

Mohamed Ameen, Laksshman Sundaram, Mengcheng Shen…·Anshul Bharat Kundaje

This study uses single-cell chromatin accessibility analysis to identify developmental trajectories and non-coding mutations associated with congenital heart disease.

110 citationstop 2%

humanscATAC-seq

𝕏 PostBluesky